EP2727975A1 - Cerium doped magnesium barium tungstate luminescent thin film, manufacturing method and application thereof - Google Patents
Cerium doped magnesium barium tungstate luminescent thin film, manufacturing method and application thereof Download PDFInfo
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- EP2727975A1 EP2727975A1 EP11868703.7A EP11868703A EP2727975A1 EP 2727975 A1 EP2727975 A1 EP 2727975A1 EP 11868703 A EP11868703 A EP 11868703A EP 2727975 A1 EP2727975 A1 EP 2727975A1
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- European Patent Office
- Prior art keywords
- thin film
- luminescent thin
- doped magnesium
- barium tungstate
- cerium doped
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- IJBYNGRZBZDSDK-UHFFFAOYSA-N barium magnesium Chemical compound [Mg].[Ba] IJBYNGRZBZDSDK-UHFFFAOYSA-N 0.000 title claims abstract description 104
- 239000010409 thin film Substances 0.000 title claims abstract description 99
- 229910052684 Cerium Inorganic materials 0.000 title claims abstract description 95
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 title claims abstract description 95
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 21
- 239000002243 precursor Substances 0.000 claims abstract description 22
- 238000005477 sputtering target Methods 0.000 claims abstract description 16
- 238000000137 annealing Methods 0.000 claims abstract description 14
- 238000005245 sintering Methods 0.000 claims abstract description 7
- 238000000034 method Methods 0.000 claims abstract description 6
- 238000001755 magnetron sputter deposition Methods 0.000 claims abstract description 5
- 238000002156 mixing Methods 0.000 claims abstract description 5
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 claims description 47
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 30
- 239000000395 magnesium oxide Substances 0.000 claims description 30
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 30
- 239000007789 gas Substances 0.000 claims description 28
- 229910000420 cerium oxide Inorganic materials 0.000 claims description 25
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 claims description 25
- 239000000758 substrate Substances 0.000 claims description 25
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- ZNOKGRXACCSDPY-UHFFFAOYSA-N tungsten trioxide Chemical group O=[W](=O)=O ZNOKGRXACCSDPY-UHFFFAOYSA-N 0.000 claims description 17
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 claims description 11
- 229910001930 tungsten oxide Inorganic materials 0.000 claims description 11
- 239000011777 magnesium Substances 0.000 claims description 10
- 238000004544 sputter deposition Methods 0.000 claims description 9
- 239000011261 inert gas Substances 0.000 claims description 4
- 238000004020 luminiscence type Methods 0.000 abstract description 6
- 238000002360 preparation method Methods 0.000 abstract description 4
- 229910000421 cerium(III) oxide Inorganic materials 0.000 abstract 1
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 14
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- 229910052786 argon Inorganic materials 0.000 description 7
- 239000010408 film Substances 0.000 description 7
- 239000011521 glass Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 239000000919 ceramic Substances 0.000 description 6
- 239000008367 deionised water Substances 0.000 description 6
- 229910021641 deionized water Inorganic materials 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 238000009832 plasma treatment Methods 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- SJPVUFMOBDBTHQ-UHFFFAOYSA-N barium(2+);dioxido(dioxo)tungsten Chemical compound [Ba+2].[O-][W]([O-])(=O)=O SJPVUFMOBDBTHQ-UHFFFAOYSA-N 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 238000002441 X-ray diffraction Methods 0.000 description 2
- 229910052788 barium Inorganic materials 0.000 description 2
- RKTYLMNFRDHKIL-UHFFFAOYSA-N copper;5,10,15,20-tetraphenylporphyrin-22,24-diide Chemical group [Cu+2].C1=CC(C(=C2C=CC([N-]2)=C(C=2C=CC=CC=2)C=2C=CC(N=2)=C(C=2C=CC=CC=2)C2=CC=C3[N-]2)C=2C=CC=CC=2)=NC1=C3C1=CC=CC=C1 RKTYLMNFRDHKIL-UHFFFAOYSA-N 0.000 description 2
- 238000001194 electroluminescence spectrum Methods 0.000 description 2
- 230000005693 optoelectronics Effects 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- -1 for example Substances 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052754 neon Inorganic materials 0.000 description 1
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
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Classifications
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01S—DEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
- H01S5/00—Semiconductor lasers
- H01S5/30—Structure or shape of the active region; Materials used for the active region
- H01S5/3018—AIIBVI compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
- C09K11/77—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals
- C09K11/7715—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals containing cerium
- C09K11/7716—Chalcogenides
- C09K11/7718—Chalcogenides with alkaline earth metals
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
- C09K11/77—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals
- C09K11/7766—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing rare earth metals containing two or more rare earth metals
- C09K11/7767—Chalcogenides
- C09K11/7768—Chalcogenides with alkaline earth metals
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/06—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
- C23C14/08—Oxides
- C23C14/081—Oxides of aluminium, magnesium or beryllium
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
- C23C14/22—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the process of coating
- C23C14/34—Sputtering
- C23C14/35—Sputtering by application of a magnetic field, e.g. magnetron sputtering
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
Definitions
- the present invention relates to the technical field of semiconductor optoelectronic materials, in particular to a cerium doped magnesium barium tungstate luminescent thin film, and manufacturing method and application thereof.
- the embodiment of the present invention provides a cerium-doped magnesium barium tungstate luminescent thin film, and manufacturing method and application thereof to solve the technical problems in the prior art, like complicated process for manufacturing a cerium-doped magnesium barium tungstate luminescent thin film, high cost, low luminescence efficiency of a cerium-doped magnesium barium tungstate luminescent thin film.
- the embodiment of the present invention further provides the use of the above-mentioned cerium doped magnesium barium tungstate luminescent thin film in electroluminescent devices.
- cerium and magnesium barium tungstate in the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention results in a film that exhibits higher luminescence efficiency, and exhibits relatively high emission peaks in both the red and blue regions, for example emission peaks at 470 nm and 670 nm; said method of manufacturing the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention presents the advantages of simplified operation, low cost, and suitable for industrial preparation.
- the embodiment of the present invention provides a cerium doped magnesium barium tungstate luminescent thin film
- Mg x Ba 1-x W 2 O 8 YCe 3+ , where x is from range of 0.13 to 0.96, preferably 0.43, Y is from range of 0.0002 to 0.0124, preferably 0.0023.
- the cerium doped magnesium barium tungstate luminescent thin film of the present invention takes magnesium barium tungstate as the luminous host material of the luminescent thin film, and takes elemental cerium as the luminescence center, which results in relatively high luminescence efficiency in the cerium doped magnesium barium tungstate luminescent thin film of the embodiment according to the present invention by making use of the combined use of magnesium barium tungstate and cerium; and renders the ability of adjusting the luminescent intensity of the cerium doped magnesium barium tungstate luminescent thin film by varying the content of magnesium and barium in the magnesium barium tungstate that acts as the luminous host material.
- figure 3 shows the EL spectra of the cerium doped magnesium barium tungstate luminescent thin film obtained from Example according to the present invention.
- the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention shows emission peaks at 470nm and 670nm.
- figure 4 shows the plot that illustrates changes of the luminescent intensity and the position of the emission peaks of the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention by varying the content of magnesium oxide.
- Curve 1 shows changes of the luminescent intensity of film
- curve 2 shows changes of the position of the emission peaks of film.
- the luminescent intensity of the cerium-doped barium magnesium tungstate luminescent film firstly increases and then decreases as the content of magnesium oxide increases. As the content in mass percentage of the magnesium oxide in the manufacturing method is about 6%, the relative luminescent intensity shows the strongest; with the increase of the content of magnesium oxide, the wavelength of the emission peaks of the cerium-doped magnesium barium tungstate luminescent film becomes shorter.
- magnesium oxide (MgO), barium oxide (BaO), tungsten oxide (WO 3 ) and cerium oxide (Ce 2 O 3 ) are powers having a purity of 99.99% or above.
- the content of magnesium oxide in mass percentage is 0.1% to 15%, preferably 2% to 10%, for example, 6%; the content of barium oxide in mass percentage is 0.1% to 40%, preferably 0.2% to 30%, for example, 30%; the content of cerium oxide in mass percentage is 0.01% to 0.8%, preferably 0.02% to 0.6%, for example, 0.15%.
- step S01 magnesium oxide, barium oxide, tungsten oxide and cerium oxide are mixed homogenously, and then sintered at a temperature of 900°C to 1300°C to form a sputtering target of ⁇ 50 ⁇ 2mm; preferably, said sintering temperature is 1250°C.
- step S02 the ITO substrate and the sputtering target are loaded into the chamber of a coating device, which the chamber is evacuated by means of a mechanical pump or a molecular pump such that a vacuum level of 1.0 ⁇ 10 -3 Pa to 1.0 ⁇ 10 -5 Pa, preferably 5.0 ⁇ 10 -4 Pa, is reached; sputtering is conducted under the following conditions: a distance of 50 to 100mm from the substrate to the target, a substrate temperature of 250°C to 750°C, employing a mixed gas of hydrogen and an inert gas as the operating gas, a gas flow rate of 15 to 30 sccm, a pressure of 0.2 to 4.5 Pa, to give a precursor of cerium doped magnesium barium tungstate luminescent thin film.
- step S02 limitations are not made there to said inert gas, for example, nitrogen, helium, argon, neon may be used; in said mixed gas of hydrogen and an inert gas, the content in volume percentage of hydrogen in said mixed gas is 1 to 15%, preferably, 10%; wherein, the distance between the substrate and the target is 70 mm, said substrate temperature is preferably 600 °C, said gas flow rate is preferably 25 sccm, said pressure is preferably 2.0Pa.
- nitrogen, helium, argon, neon may be used
- the content in volume percentage of hydrogen in said mixed gas is 1 to 15%, preferably, 10%
- the distance between the substrate and the target is 70 mm
- said substrate temperature is preferably 600 °C
- said gas flow rate is preferably 25 sccm
- said pressure is preferably 2.0Pa.
- step S03 the precursor of cerium doped magnesium barium tungstate luminescent thin film is subjected to annealing in a vacuum furnace at a pressure of 0.01Pa for 1 to 3 h, preferably 2 h, where the annealing temperature is 500°C to 800°C, preferably 700 °C, to give a cerium doped magnesium barium tungstate luminescent thin film.
- the method of manufacturing the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention by mixing magnesium oxide, barium oxide, tungsten oxide and cerium oxide, sintering for forming sputtering target, followed by sputtering for forming film provides the cerium doped magnesium barium tungstate luminescent thin film.
- Said cerium doped magnesium barium tungstate luminescent thin film exhibits relative high luminescence efficiency; said method of manufacturing the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention presents the advantages of simplified operation, less cost, and suitable for industrial preparation.
- the embodiment of the present invention further provides the use of said cerium doped magnesium barium tungstate luminescent thin film in electroluminescent devices.
- figure 5 shows schematically the structure of an electroluminescent device which employs the cerium doped magnesium barium tungstate luminescent thin film of the embodiment according to the present invention, which comprises anode 1, emission layer 2 and cathode 3.
- the material for said anode 1 is ITO coated glass
- the material for said emission layer 2 is the cerium doped magnesium barium tungstate luminescent thin film of the embodiment according to the present invention
- the material for said cathode 3 is silver.
- cerium doped magnesium barium tungstate luminescent thin film is then deposited a layer of Ag as a cathode, to give an electroluminescent device comprising the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention.
- figure 2 shows the XRD patterns of the cerium doped magnesium barium tungstate luminescent thin film obtained from Example 1 according to the present invention, which, as compared with standard PDF card, corresponds to the crystallization peaks of barium tungstate, whereas diffraction peaks are not found for the doping elements and other impurities.
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Abstract
Description
- The present invention relates to the technical field of semiconductor optoelectronic materials, in particular to a cerium doped magnesium barium tungstate luminescent thin film, and manufacturing method and application thereof.
- Scheelite structured AWO4 (A = Ca, Sr, Ba) is one important type of laser materials. It presents as a tetragonal structure at room temperature and emits blue light under ultraviolet ray excitation. Barium tungstate maintains its tetragonal structure from room temperature to its melting point (1820 K), and possesses good structural stability. Due to these excellent properties, barium tungstate has an attractive applicable prospect in the field of light emitting and display technology, laser and optoelectronics technology and detection technology. At present, barium tungstate has been applied to phosphors, but less involved in the field of cerium-doped magnesium barium tungstate luminescent thin film, and the resulting film exhibits low luminescence efficiency; further, complicated preparation process is often involved.
- In view of this, the embodiment of the present invention provides a cerium-doped magnesium barium tungstate luminescent thin film, and manufacturing method and application thereof to solve the technical problems in the prior art, like complicated process for manufacturing a cerium-doped magnesium barium tungstate luminescent thin film, high cost, low luminescence efficiency of a cerium-doped magnesium barium tungstate luminescent thin film.
- The embodiment of the present invention is achieved in the following way:
- providing a cerium-doped magnesium barium tungstate luminescent thin film,
- having the molecular formula of MgxBa1-xW2O8: YCe3+, where x is from range of 0.13 to 0.96, Y is from range of 0.0002 to 0.0124;
- and
- providing a method for manufacturing a cerium-doped magnesium barium tungstate luminescent thin film, comprising the following steps:
- mixing magnesium oxide, barium oxide, tungsten oxide and cerium oxide; sintering for forming sputtering target, wherein the content in mass percentage of said magnesium oxide is 0.1% to 15%, the content in mass percentage of said barium oxide is 0.1% to 40%, the content in mass percentage of said cerium oxide is 0.01% to 0.8%, the rest is tungsten trioxide;
- forming the precursor of cerium doped magnesium barium tungstate luminescent thin film by subjecting the sputtering target to magnetron sputtering;
- annealing the precursor of cerium doped magnesium barium tungstate luminescent thin film to form the cerium doped magnesium barium tungstate luminescent thin film.
- The embodiment of the present invention further provides the use of the above-mentioned cerium doped magnesium barium tungstate luminescent thin film in electroluminescent devices.
- The combined use of cerium and magnesium barium tungstate in the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention results in a film that exhibits higher luminescence efficiency, and exhibits relatively high emission peaks in both the red and blue regions, for example emission peaks at 470 nm and 670 nm; said method of manufacturing the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention presents the advantages of simplified operation, low cost, and suitable for industrial preparation.
-
-
Figure 1 shows the flowchart of the manufacturing method of the cerium doped magnesium barium tungstate luminescent thin film of the embodiment according to the present invention. -
Figure 2 shows the XRD patterns of the cerium doped magnesium barium tungstate luminescent thin film obtained from Example 1 according to the present invention. -
Figure 3 shows the EL spectra of the cerium doped magnesium barium tungstate luminescent thin film obtained from Example according to the present invention. -
Figure 4 shows the plot that illustrates the correlation of the luminescent intensity and the position of the emission peaks of the cerium doped magnesium barium tungstate luminescent thin film with the content of magnesium oxide. -
Figure 5 shows schematically the structure of an electroluminescent device which employs the cerium doped magnesium barium tungstate luminescent thin film of the embodiment according to the present invention. - The above and other objects, features, and advantages of the present invention will become more apparent from the following detailed description when taken in conjunction with the accompanying drawings and embodiments. It should be understood that the specific embodiments described herein are merely for illustrative purpose, rather than limiting the present invention.
- The embodiment of the present invention provides a cerium doped magnesium barium tungstate luminescent thin film,
- having the molecular formula of MgxBa1-xW2O8: YCe3+, where x is from range of 0.13 to 0.96, preferably 0.43, Y is from range of 0.0002 to 0.0124, preferably 0.0023.
- The cerium doped magnesium barium tungstate luminescent thin film of the present invention takes magnesium barium tungstate as the luminous host material of the luminescent thin film, and takes elemental cerium as the luminescence center, which results in relatively high luminescence efficiency in the cerium doped magnesium barium tungstate luminescent thin film of the embodiment according to the present invention by making use of the combined use of magnesium barium tungstate and cerium; and renders the ability of adjusting the luminescent intensity of the cerium doped magnesium barium tungstate luminescent thin film by varying the content of magnesium and barium in the magnesium barium tungstate that acts as the luminous host material.
- With reference to
figure 3, figure 3 shows the EL spectra of the cerium doped magnesium barium tungstate luminescent thin film obtained from Example according to the present invention. As shown infigure 3 , the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention shows emission peaks at 470nm and 670nm. With reference tofigure 4, figure 4 shows the plot that illustrates changes of the luminescent intensity and the position of the emission peaks of the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention by varying the content of magnesium oxide.Curve 1 shows changes of the luminescent intensity of film,curve 2 shows changes of the position of the emission peaks of film. As shown infigure 4 , the luminescent intensity of the cerium-doped barium magnesium tungstate luminescent film firstly increases and then decreases as the content of magnesium oxide increases. As the content in mass percentage of the magnesium oxide in the manufacturing method is about 6%, the relative luminescent intensity shows the strongest; with the increase of the content of magnesium oxide, the wavelength of the emission peaks of the cerium-doped magnesium barium tungstate luminescent film becomes shorter. - See
figure 1 , a flowchart of the manufacturing method of the cerium doped magnesium barium tungstate luminescent thin film of the embodiment according to the present invention is shown, said method comprises the steps of: - step S01, manufacturing of the sputtering target
- mixing magnesium oxide, barium oxide, tungsten oxide and cerium oxide; sintering for forming sputtering target, wherein the content in mass percentage of said magnesium oxide is 0.1% to 15%, the content in mass percentage of said barium oxide is 0.1% to 40%, the content in mass percentage of said cerium oxide is 0.01% to 0.8%, the rest is tungsten trioxide;
- step S02, magnetron sputtering
- forming the precursor of cerium doped magnesium barium tungstate luminescent thin film by subjecting the sputtering target to magnetron sputtering;
- step S03, annealing
- annealing the precursor of cerium doped magnesium barium tungstate luminescent thin film to form the cerium doped magnesium barium tungstate luminescent thin film.
- Specifically, in step S01, magnesium oxide (MgO), barium oxide (BaO), tungsten oxide (WO3) and cerium oxide (Ce2O3) are powers having a purity of 99.99% or above. The content of magnesium oxide in mass percentage is 0.1% to 15%, preferably 2% to 10%, for example, 6%; the content of barium oxide in mass percentage is 0.1% to 40%, preferably 0.2% to 30%, for example, 30%; the content of cerium oxide in mass percentage is 0.01% to 0.8%, preferably 0.02% to 0.6%, for example, 0.15%.
- In step S01, magnesium oxide, barium oxide, tungsten oxide and cerium oxide are mixed homogenously, and then sintered at a temperature of 900°C to 1300°C to form a sputtering target of Φ50×2mm; preferably, said sintering temperature is 1250°C.
- Specifically, in step S02, the ITO substrate and the sputtering target are loaded into the chamber of a coating device, which the chamber is evacuated by means of a mechanical pump or a molecular pump such that a vacuum level of 1.0 × 10-3 Pa to 1.0 × 10-5 Pa, preferably 5.0 × 10-4 Pa, is reached; sputtering is conducted under the following conditions: a distance of 50 to 100mm from the substrate to the target, a substrate temperature of 250°C to 750°C, employing a mixed gas of hydrogen and an inert gas as the operating gas, a gas flow rate of 15 to 30 sccm, a pressure of 0.2 to 4.5 Pa, to give a precursor of cerium doped magnesium barium tungstate luminescent thin film.
- In step S02, limitations are not made there to said inert gas, for example, nitrogen, helium, argon, neon may be used; in said mixed gas of hydrogen and an inert gas, the content in volume percentage of hydrogen in said mixed gas is 1 to 15%, preferably, 10%; wherein, the distance between the substrate and the target is 70 mm, said substrate temperature is preferably 600 °C, said gas flow rate is preferably 25 sccm, said pressure is preferably 2.0Pa.
- Specifically, in step S03, the precursor of cerium doped magnesium barium tungstate luminescent thin film is subjected to annealing in a vacuum furnace at a pressure of 0.01Pa for 1 to 3 h, preferably 2 h, where the annealing temperature is 500°C to 800°C, preferably 700 °C, to give a cerium doped magnesium barium tungstate luminescent thin film.
- The method of manufacturing the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention by mixing magnesium oxide, barium oxide, tungsten oxide and cerium oxide, sintering for forming sputtering target, followed by sputtering for forming film provides the cerium doped magnesium barium tungstate luminescent thin film. Said cerium doped magnesium barium tungstate luminescent thin film exhibits relative high luminescence efficiency; said method of manufacturing the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention presents the advantages of simplified operation, less cost, and suitable for industrial preparation.
- The embodiment of the present invention further provides the use of said cerium doped magnesium barium tungstate luminescent thin film in electroluminescent devices. With reference to
figure 5, figure 5 shows schematically the structure of an electroluminescent device which employs the cerium doped magnesium barium tungstate luminescent thin film of the embodiment according to the present invention, which comprisesanode 1,emission layer 2 andcathode 3. The material for saidanode 1 is ITO coated glass, the material for saidemission layer 2 is the cerium doped magnesium barium tungstate luminescent thin film of the embodiment according to the present invention and the material for saidcathode 3 is silver. - Detailed description to said cerium doped magnesium barium tungstate luminescent thin film will now be given with reference to the exemplary embodiments:
-
- Magnesium oxide, barium oxide, tungsten oxide and cerium oxide are mixed homogenously, wherein the content in mass percentage of MgO is 6%, the content in mass percentage of BaO is 30%, the content in mass percentage of Ce2O3 is 0.15%, the rest is WO3 (in mass percentage);
- The mixture is sintered at a temperature of 1250°C to form a ceramic sputtering target of Φ50 × 2mm;
- The target is loaded into a vacuum chamber, and the ITO coated glass substrate is then subjected to ultrasonic washing with a sequential use of acetone, anhydrous ethanol and deionized water, which is then subjected to oxygen plasma treatment, followed by placing it into the vacuum chamber. The distance between the target and the substrate is set to 75 mm. The chamber is evacuated by means of a mechanical pump and molecular pump such that a vacuum level 5.0 × 10-4 Pa is reached, to which the vacuum chamber is purged with a mixed gas of argon and hydrogen as the operating gas, where the hydrogen content is 10% (in volume percentage), the gas flow rate is 25 sccm, the pressure is adjusted to 2.0 Pa, the substrate temperature is 600°C, a precursor of cerium doped magnesium barium tungstate luminescent thin film is formed by sputtering;
- the precursor of cerium doped magnesium barium tungstate luminescent thin film is subjected to annealing in a vacuum furnace at 0.01Pa under a temperature of 700 °C for 2 h to form the cerium doped magnesium barium tungstate luminescent thin film.
- The thus obtained cerium doped magnesium barium tungstate luminescent thin film has a molecular formula of: Mg0.43Ba0.57W2O8:0.0023 Ce3+;
- Onto the cerium doped magnesium barium tungstate luminescent thin film is then deposited a layer of Ag as a cathode, to give an electroluminescent device comprising the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention.
- With reference to
figure 2, figure 2 shows the XRD patterns of the cerium doped magnesium barium tungstate luminescent thin film obtained from Example 1 according to the present invention, which, as compared with standard PDF card, corresponds to the crystallization peaks of barium tungstate, whereas diffraction peaks are not found for the doping elements and other impurities. -
- Magnesium oxide, barium oxide, tungsten oxide and cerium oxide are mixed homogenously, wherein the content in mass percentage of MgO is 0.1%, the content in mass percentage of BaO is 40%, the content in mass percentage of Ce2O3 is 0.01%, the rest is WO3 (in mass percentage);
- The mixture is sintered at a temperature of 900°C to form a ceramic sputtering target of Φ 50 × 2mm;
- The target is loaded into a vacuum chamber, and the ITO coated glass substrate is then subjected to ultrasonic washing with a sequential use of acetone, anhydrous ethanol and deionized water, which is then subjected to oxygen plasma treatment, followed by placing it into the vacuum chamber. The distance between the target and the substrate is set to 50 mm. The chamber is evacuated by means of a mechanical pump and molecular pump such that a vacuum level 1.0 × 10-5 Pa is reached, to which the vacuum chamber is purged with a mixed gas of argon and hydrogen as the operating gas, where the hydrogen content is 1% (in volume percentage), the gas flow rate is 15 sccm, the pressure is adjusted to 0.2 Pa, the substrate temperature is 600°C, a precursor of cerium doped magnesium barium tungstate luminescent thin film is formed by sputtering;
- the precursor of cerium doped magnesium barium tungstate luminescent thin film is subjected to annealing in a vacuum furnace at 0.01Pa under a temperature of 500 °C for 1 h to form the cerium doped magnesium barium tungstate luminescent thin film.
- The thus obtained cerium doped magnesium barium tungstate luminescent thin film has a molecular formula of: Mg0.13Ba0.87W2O8:0.0002 Ce3+;
- Onto the cerium doped magnesium barium tungstate luminescent thin film is then deposited a layer of Ag as a cathode, to give an electroluminescent device comprising the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention.
-
- Magnesium oxide, barium oxide, tungsten oxide and cerium oxide are mixed homogenously, wherein the content in mass percentage of MgO is 15%, the content in mass percentage of BaO is 0.1%, the content in mass percentage of Ce2O3 is 0.8%, the rest is WO3 (in mass percentage);
- The mixture is sintered at a temperature of 1300°C to form a
ceramic sputtering target 50 × 2mm; - The target is loaded into a vacuum chamber, and the ITO coated glass substrate is then subjected to ultrasonic washing with a sequential use of acetone, anhydrous ethanol and deionized water, which is then subjected to oxygen plasma treatment, followed by placing it into the vacuum chamber. The distance between the target and the substrate is set to 100 mm. The chamber is evacuated by means of a mechanical pump and molecular pump such that a vacuum level 1.0 × 10-3 Pa is reached, to which the vacuum chamber is purged with a mixed gas of argon and hydrogen as the operating gas, where the hydrogen content is 15% (in volume percentage), the gas flow rate is 30 sccm, the pressure is adjusted to 4.5 Pa, the substrate temperature is 600°C, a precursor of cerium doped magnesium barium tungstate luminescent thin film is formed by sputtering;
- the precursor of cerium doped magnesium barium tungstate luminescent thin film is subjected to annealing in a vacuum furnace at 0.01Pa under a temperature of 800 °C for 3 h to form the cerium doped magnesium barium tungstate luminescent thin film.
- The thus obtained cerium doped magnesium barium tungstate luminescent thin film has a molecular formula of: Mg0.96Ba0.04W2O8:0.0124 Ce3+;
- Onto the cerium doped magnesium barium tungstate luminescent thin film is then deposited a layer of Ag as a cathode, to give an electroluminescent device comprising the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention.
-
- Magnesium oxide, barium oxide, tungsten oxide and cerium oxide are mixed homogenously, wherein the content in mass percentage of MgO is 0.2%, the content in mass percentage of BaO is 30%, the content in mass percentage of Ce2O3 is 0.6%, the rest is WO3 (in mass percentage);
- The mixture is sintered at a temperature of 900°C to form a ceramic sputtering target of Φ50×2mm;
- The target is loaded into a vacuum chamber, and the ITO coated glass substrate is then subjected to ultrasonic washing with a sequential use of acetone, anhydrous ethanol and deionized water, which is then subjected to oxygen plasma treatment, followed by placing it into the vacuum chamber. The distance between the target and the substrate is set to 50 mm. The chamber is evacuated by means of a mechanical pump and molecular pump such that a vacuum level 5.0 × 10-4 Pa is reached, to which the vacuum chamber is purged with a mixed gas of argon and hydrogen as the operating gas, where the hydrogen content is 8% (in volume percentage), the gas flow rate is 20 sccm, the pressure is adjusted to 0.2 Pa, the substrate temperature is 600°C, a precursor of cerium doped magnesium barium tungstate luminescent thin film is formed by sputtering;
- the precursor of cerium doped magnesium barium tungstate luminescent thin film is subjected to annealing in a vacuum furnace at 0.01Pa under a temperature of 500 °C for 2 h to form the cerium doped magnesium barium tungstate luminescent thin film.
- The thus obtained cerium doped magnesium barium tungstate luminescent thin film has a molecular formula of: Mg0.026Ba0.974W2O8:0.0093Ce3+;
- Onto the cerium doped magnesium barium tungstate luminescent thin film is then deposited a layer of Ag as a cathode, to give an electroluminescent device comprising the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention.
-
- Magnesium oxide, barium oxide, tungsten oxide and cerium oxide are mixed homogenously, wherein the content in mass percentage of MgO is 10%, the content in mass percentage of BaO is 0.2%, the content in mass percentage of Ce2O3 is 0.4%, the rest is WO3 (in mass percentage);
- The mixture is sintered at a temperature of 1300°C to form a
ceramic sputtering target 50 × 2mm; - The target is loaded into a vacuum chamber, and the ITO coated glass substrate is then subjected to ultrasonic washing with a sequential use of acetone, anhydrous ethanol and deionized water, which is then subjected to oxygen plasma treatment, followed by placing it into the vacuum chamber. The distance between the target and the substrate is set to 80 mm. The chamber is evacuated by means of a mechanical pump and molecular pump such that a vacuum level 5.0 × 10-4 Pa is reached, to which the vacuum chamber is purged with a mixed gas of argon and hydrogen as the operating gas, where the hydrogen content is 11% (in volume percentage), the gas flow rate is 23 sccm, the pressure is adjusted to 2.0 Pa, the substrate temperature is 600°C, a precursor of cerium doped magnesium barium tungstate luminescent thin film is formed by sputtering;
- the precursor of cerium doped magnesium barium tungstate luminescent thin film is subjected to annealing in a vacuum furnace at 0.01Pa under a temperature of 650°C for 2 h to form the cerium doped magnesium barium tungstate luminescent thin film.
- The thus obtained cerium doped magnesium barium tungstate luminescent thin film has a molecular formula of: Mg0.995Ba0.005W2O8:0.0062Ce3+;
- Onto the cerium doped magnesium barium tungstate luminescent thin film is then deposited a layer of Ag as a cathode, to give an electroluminescent device comprising the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention.
-
- Magnesium oxide, barium oxide, tungsten oxide and cerium oxide are mixed homogenously, wherein the content in mass percentage of MgO is 15%, the content in mass percentage of BaO is 20%, the content in mass percentage of Ce2O3 is 0.8%, the rest is WO3 (in mass percentage);
- The mixture is sintered at a temperature of 1000°C to form a
ceramic sputtering target 50 × 2mm; - The target is loaded into a vacuum chamber, and the ITO coated glass substrate is then subjected to ultrasonic washing with a sequential use of acetone, anhydrous ethanol and deionized water, which is then subjected to oxygen plasma treatment, followed by placing it into the vacuum chamber. The distance between the target and the substrate is set to 95 mm. The chamber is evacuated by means of a mechanical pump and molecular pump such that a vacuum level 5.0 × 10-4 Pa is reached, to which the vacuum chamber is purged with a mixed gas of argon and hydrogen as the operating gas, where the hydrogen content is 9% (in volume percentage), the gas flow rate is 20 sccm, the pressure is adjusted to 2.0 Pa, the substrate temperature is 600°C, a precursor of cerium doped magnesium barium tungstate luminescent thin film is formed by sputtering;
- the precursor of cerium doped magnesium barium tungstate luminescent thin film is subjected to annealing in a vacuum furnace at 0.01Pa under a temperature of 750 °C for 2.5 h to form the cerium doped magnesium barium tungstate luminescent thin film.
- The thus obtained cerium doped magnesium barium tungstate luminescent thin film has a molecular formula of: Mg0.74Ba0.26W2O8:0.0124Ce3+;
- Onto the cerium doped magnesium barium tungstate luminescent thin film is then deposited a layer of Ag as a cathode, to give an electroluminescent device comprising the cerium doped magnesium barium tungstate luminescent thin film of the embodiment of the present invention.
- Although the present invention has been described and illustrated in detail, it is clearly understood that the same is by way of illustrating the preferred embodiment of the present invention and is not to be taken by way of limitation, it should be understood that various changes, substitutions, and alterations could be made hereto without departing from the spirit and scope of the invention.
Claims (10)
- A cerium doped magnesium barium tungstate luminescent thin film, characterized in that said cerium doped magnesium barium tungstate luminescent thin film has the molecular formula of MgxBa1-xW2O8: YCe3+, where x is from range of 0.13 to 0.96, Y is from range of 0.0002 to 0.0124.
- A cerium doped magnesium barium tungstate luminescent thin film according to claim 1, characterized in that x is 0.43, Y is 0.0023.
- A method of manufacturing a cerium doped magnesium barium tungstate luminescent thin film, characterized in that said method comprises the steps of: mixing magnesium oxide, barium oxide, tungsten oxide and cerium oxide; sintering for forming sputtering target, wherein the content in mass percentage of said magnesium oxide is 0.1% to 15%, the content in mass percentage of said barium oxide is 0.1% to 40%, the content in mass percentage of said cerium oxide is 0.01% to 0.8%, the rest is tungsten trioxide; forming the precursor of cerium doped magnesium barium tungstate luminescent thin film by magnetron sputtering; annealing the precursor of cerium doped magnesium barium tungstate luminescent thin film to obtain the cerium doped magnesium barium tungstate luminescent thin film.
- A method of manufacturing a cerium doped magnesium barium tungstate luminescent thin film according to claim 3, characterized in that the content in mass percentage of said magnesium oxide is 0.2% to 10%, the content in mass percentage of said barium oxide is 0.2% to 30%, the content in mass percentage of said cerium oxide is 0.02% to 0.6%, the rest is tungsten trioxide.
- A method of manufacturing a cerium doped magnesium barium tungstate luminescent thin film according to claim 3, characterized in that the content in mass percentage of said magnesium oxide is 6%, the content in mass percentage of said barium oxide is 30%, the content in mass percentage of said cerium oxide is 0.15%, the rest is tungsten trioxide.
- A method of manufacturing a cerium doped magnesium barium tungstate luminescent thin film according to claim 3, characterized in that said sintering is conducted at a temperature of 900°C to 1300°C.
- A method of manufacturing a cerium doped magnesium barium tungstate luminescent thin film according to claim 3, characterized in that said sputtering is conducted under the following conditions: the distance between the substrate and the target is 50 to 100 mm, the substrate temperature is 250°C to 750°C, employing a mixed gas of hydrogen and an inert gas as the operating gas, gas flow rate is 15 to 30sccm, pressure is 0.2 to 4.5Pa.
- A method of manufacturing a cerium doped magnesium barium tungstate luminescent thin film according to claim 7, characterized in that the content in volume percentage of hydrogen in said mixed gas is 1% to 15%.
- A method of manufacturing a cerium doped magnesium barium tungstate luminescent thin film according to claim 3, characterized in that said annealing is conducted at a temperature of 500°C to 800°C for a time period of 1 to 3 h.
- A use of a cerium doped magnesium barium tungstate luminescent thin film according to claim 1 or 2 in electroluminescent devices.
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3257327A (en) * | 1962-05-07 | 1966-06-21 | Bell Telephone Labor Inc | Process for growing neodymium doped single crystal divalent metal ion tungstates |
US20050214573A1 (en) * | 2004-03-26 | 2005-09-29 | Canon Kabushiki Kaisha | Light-emitting material and light-emitting element |
US20100244066A1 (en) * | 2009-03-27 | 2010-09-30 | Chunghwa Picture Tubes, Ltd. | Red light fluorescent material and manufacturing method thereof, and white light luminescent device |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3338841A (en) * | 1964-05-14 | 1967-08-29 | Du Pont | Luminescent molybdate and tungstate compositions |
JPS5821477A (en) * | 1981-07-31 | 1983-02-08 | Yoshihide Kodera | Fluorescent material |
JPH01263188A (en) * | 1988-04-15 | 1989-10-19 | Hitachi Ltd | Calcium tungstate luminescent thin layer and its production |
JPH05320639A (en) * | 1992-05-25 | 1993-12-03 | Konica Corp | Electroluminescent element and its production |
JPH06251872A (en) | 1993-02-23 | 1994-09-09 | Konica Corp | Electroluminescent element and its manufacture |
JPH0892553A (en) * | 1994-09-19 | 1996-04-09 | Toshiba Corp | Fluorescent substance |
US20030052000A1 (en) * | 1997-07-11 | 2003-03-20 | Vladimir Segal | Fine grain size material, sputtering target, methods of forming, and micro-arc reduction method |
JP3769609B2 (en) | 2001-11-06 | 2006-04-26 | 国立大学法人長岡技術科学大学 | High-brightness metal oxide fluorescent structure, manufacturing method and manufacturing apparatus thereof |
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JP4378230B2 (en) | 2004-06-15 | 2009-12-02 | キヤノン株式会社 | Light emitting device and manufacturing method thereof |
JP2006232601A (en) | 2005-02-24 | 2006-09-07 | Osaka Univ | Yellow pigment |
WO2006111568A2 (en) * | 2005-04-20 | 2006-10-26 | Etech Ag | Novel materials used for emitting light |
CN100395380C (en) | 2006-04-21 | 2008-06-18 | 北京工业大学 | Process for preparing barium tungstate single crystal with improved doping concentration of rare earth ion |
WO2009096165A1 (en) * | 2008-01-31 | 2009-08-06 | Panasonic Corporation | Optical information recording medium, method for manufacturing the same, and target thereof |
CN103233204A (en) * | 2008-06-06 | 2013-08-07 | 出光兴产株式会社 | Sputtering target for oxide thin film and method for producing same |
CN101368258A (en) | 2008-09-12 | 2009-02-18 | 江苏大学 | Preparation method of negative thermal expansion material ZrW2O8 film |
CN102791052B (en) * | 2011-05-16 | 2015-03-18 | 海洋王照明科技股份有限公司 | Titanium cerium co-doped barium tungstate light-emitting film, preparation method thereof and organic light-emitting device |
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Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3257327A (en) * | 1962-05-07 | 1966-06-21 | Bell Telephone Labor Inc | Process for growing neodymium doped single crystal divalent metal ion tungstates |
US20050214573A1 (en) * | 2004-03-26 | 2005-09-29 | Canon Kabushiki Kaisha | Light-emitting material and light-emitting element |
US20100244066A1 (en) * | 2009-03-27 | 2010-09-30 | Chunghwa Picture Tubes, Ltd. | Red light fluorescent material and manufacturing method thereof, and white light luminescent device |
Non-Patent Citations (1)
Title |
---|
See also references of WO2013000117A1 * |
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